BEUDAMED
    12 results · 18ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    KSEA ENDO TIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Medtronic Reusable Instruments

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902575464·INSTRUMENT 8981130 SNGL PRONG P 30MM BTM

    OMEGA

    FDA UDI
    Stryker GmbH·07613154482825·X-Ray Template Supracondylar Plate Lag Screw 9...

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981130·anteriors; shade A4; mould UL4

    Symmetry

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482033241·Symmetry® Forceps, Mckernan Tri-Grasping, Fenes...

    BRIDGEPOINT MEDICAL CROSSBOSS PERCUTANEOUS CORONARY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Powder Free Blue Nitrile Examination Gloves, Tested for Use with Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ETEST FOSFOMYCIN FM 1024 WW B30

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code JWY·April 16, 2020

    UMBILICAL CATHETER

    FDA Adverse Event
    Malfunction ·VYGON·Product code FOS·February 17, 2021

    LEAD MODEL 304

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·February 27, 2013

    BIOMET SHOULDER JOINT REPLACEMENT PROSTHESES

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·February 3, 2011

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 5, 2014